A field emitter comprising a conductive metal and a diamond emission tip with negative electron affinity in ohmic contact with and protruding above the metal. The field emitter is fabricated by coating a substrate with an insulating diamond film having negative electron affinity and a top surface with spikes and valleys, depositing a conductive metal on the diamond film, and applying an etch to expose the spikes without exposing the valleys, thereby forming diamond emission tips which protrude a height above the conductive metal less than the mean free path of electrons in the diamond film.

Patent
   5341063
Priority
Nov 07 1991
Filed
Nov 24 1992
Issued
Aug 23 1994
Expiry
Nov 07 2011
Assg.orig
Entity
Large
55
23
all paid
1. A field emitter, comprising:
a conductive metal; and
a diamond emission tip composed entirely of exposed diamond with negative electron affinity in contact with and protruding above a substantially planar top surface of said metal wherein said diamond emission tip extends from a diamond film beneath said conductive metal.
11. A field emitter, comprising:
a substrate;
a diamond film on said substrate, said diamond film having negative electron affinity and comprising a surface with spikes and valleys; and
a conductive metal on said surface of said diamond film, said conductive metal covering said valleys and lower portions of said spikes wherein upper portions of said spikes protrude above a substantially planar top surface of said conductive metal to form diamond emission tips composed entirely of exposed diamond.
10. A field emitter, comprising:
a substrate;
a conductive metal on said substrate; and
a plurality of insulating diamond emission tips composed entirely of exposed diamond having an electron affinity in the range of approximately -1.2 to -0.2 electron volts annealed to and in ohmic contact with said conductive metal and protruding above a substantially planar top surface of said conductive metal by a height less than the mean free path of electrons in said diamond emission tips wherein said diamond emission tips extend from a diamond film beneath said conductive metal.
25. A field emitter, comprising:
a substrate;
a diamond film on said substrate, said diamond film having negative electron affinity and comprising a top surface with sharp vertical spikes surrounded by valleys; and
a conductive metal in contact with and covering said valleys and lower portions of said spikes, wherein upper portions of said spikes protrude above a substantially planar top surface of said conductive metal to form diamond emission tips composed entirely of exposed diamond, said diamond emission tips having a height less than the mean free path of electrons in said diamond film thereby allowing electrons in said conductive metal to ballistically tunnel through said diamond emission tips.
28. A field emitter, comprising:
a substrate;
a diamond film on said substrate, said diamond film being undoped and insulating, having negative electron affinity and comprising a top surface composed of sharp vertical spikes consisting of upper and lower portions surrounded by valleys; and
a conductive metal in ohmic contact with and covering said valleys and said lower portions of said spikes, wherein said upper portions of said spikes protrude above a substantially planer top surface of said conductive metal to form diamond emission tips composed entirely of exposed diamond, said diamond emission tips having a height less than the mean free path of electrons in said diamond film thereby allowing electrons in said conductive metal to ballistically tunnel through said diamond emission tips.
2. The field emitter of claim 1 with said diamond emission tip having a (111) orientation and an electron affinity in the range of approximately -1.2 to -0.2 electron volts.
3. The field emitter of claim 1 with said diamond emission tip being insulating and protruding a height above said conductive metal less than the mean free path of electrons in said diamond emission tip.
4. The field emitter of claim 3 with said height between approximately 10 to 100 angstroms.
5. The field emitter of claim 4 with said height between approximately 20 to 50 angstroms.
6. The field emitter of claim 1 with said conductive metal annealed to said diamond emission tip.
7. The field emitter of claim 6 with said diamond emission tip being insulating and protruding a height above said conductive metal less than the mean free path of electrons in said diamond emission tip.
8. The field emitter of claim 7 with a substrate beneath said conductive metal.
9. The field emitter of claim 8 with said conductive metal being titanium or tungsten.
12. The field emitter of claim 11 with said substrate is selected from the group consisting of glass or quartz.
13. The field emitter of claim 11 with said diamond film being undoped and insulating.
14. The field emitter of claim 11 with said diamond film having a (111) orientation.
15. The field emitter of claim 11 with the thickness of said diamond film in the range of approximately 500 to 5,000 angstroms.
16. The field emitter of claim 11 with said diamond film having an electron affinity in the range of approximately -1.2 to -0.2 electron volts.
17. The field emitter of claim 11 with said diamond emission tips protruding a height above said conductive metal less than the mean free path of electrons in said diamond film thereby allowing electrons to ballistically tunnel through said diamond emission tips.
18. The field emitter of claim 17 with said height between approximately 10 to 100 angstroms.
19. The field emitter of claim 18 with said height between approximately 20 to 50 angstroms.
20. The field emitter of claim 11 with said diamond emission tips being horizontally spaced by less than 1 micron.
21. The field emitter of claim 11 with said conductive metal being titanium or tungsten.
22. The field emitter of claim 11 with said conductive metal in ohmic contact with said diamond film.
23. The field emitter of claim 11 with said conductive metal annealed to said diamond film.
24. The field emitter of claim 11 with an alloy of said conductive metal and said diamond film at the interface therebetween.
26. The field emitter of claim 25 wherein said diamond film is undoped and insulating, and said diamond film is annealed to said conductive metal.
27. The filed emitter of claim 26 wherein said diamond film is in ohmic contact with said conductive metal.

This is a divisional of U.S. Ser. No. 07/789,237 filed Nov. 7, 1991 now U.S. Pat. No. 5,199,918.

1. Field of the Invention

The invention relates to field emitters, and more particularly to a field emitter with diamond emission tips and method of making same.

2. Description of Related Art

Field emitters are widely used in ordinary and scanning electron microscopes since emission is affected by the adsorbed materials. Field emitters have also been found useful in flat panel displays and vacuum microelectronics applications. Cold cathode and field emission based flat panel displays have several advantages over other types of flat panel displays, including low power dissipation, high intensity and low projected cost. Thus, an improved field emitter and any process which reduces the complexity of fabricating field emitters is clearly useful.

The present invention can be better appreciated with an understanding of the related physics. General electron emission can be analogized to the ionization of a free atom. Prior to ionization, the energy of electrons in an atom is lower than electrons at rest in a vacuum. In order to ionize the atom, energy must be supplied to the electrons in the atom. That is, the atom fails to spontaneously emit electrons unless the electrons are provided with energy greater than or equal to the electrons at rest in the vacuum. Energy can be provided by numerous means, such as by heat or irradiation with light. When sufficient energy is imparted to the atom, ionization occurs and the atom releases one or more electrons.

Several types of electron emissions are known. Thermionic emission involves an electrically charged particle emitted by an incandescent substance (as in a vacuum tube or incandescent light bulb). Photoemission releases electrons from a material by means of energy supplied by incidence of radiation, especially light. Secondary emission occurs by bombardment of a substance with charged particles such as electrons or ions. Electron injection involves the emission from one solid to another. Finally, field emission refers to the emission of electrons due to an electric field.

In field emission (or cold emission), electrons under the influence of a strong electric field are liberated out of a substance (usually a metal or semiconductor) into a dielectric (usually a vacuum). The electrons "tunnel" through a potential barrier instead of escaping "over" it as in thermionics or photoemission. Field emission is therefore a quantum-mechanics phenomena with no classical analog. A more detailed discussion of the physics of field emission can be found in U.S. Pat. No. 4,663,559 to Christensen; Cade and Lee, "Vacuum Microelectronics", GEC J. Res. Inc., Marconi Rev., 7(3), 129 (1990); and Cutler and Tsong, Field Emission and Related Topics (1978).

The shape of a field emitter affects its emission characteristics. Field emission is most easily obtained from sharply pointed needles or tips whose ends have been smoothed into a nearly hemispherical shape by heating. Tip radii as small as 100 nanometers have been reported. As an electric field is applied, the electric lines of force diverge radially from the tip and the emitted electron trajectories initially follow these lines of force. Field emitters with such sharp features similar to a "Spindt cathode" have been previously invented. An overview of vacuum electronics and Spindt type cathodes is found in the November and December, 1989 issues of IEEE Transactions of Electronic Devices. Fabrication of such fine tips, however, normally requires extensive fabrication facilities to finely tailor the emitter into a conical shape. Further, it is difficult to build large area field emitters since the cone size is limited by the lithographic equipment. It is also difficult to perform fine feature lithography on large area substrates as required by flat panel display type applications. Thus, there is a need for a method of making field emitters with fine conical or pyramid shaped features without the use of lithography.

The electron affinity (also called work function) of the electron emitting surface or tip of a field emitter also affects emission characteristics. Electron affinity is the voltage (or energy) required to extract or emit electrons from a surface. The lower the electron affinity, the lower the voltage required to produce a particular amount of emission. If the electron affinity is negative then the surface shall spontaneously emit electrons until stopped by space charge, although the space charge can be overcome by applying a small voltage, e.g. 5 volts. Compared to the 10,000 to 20,000 volts normally required to achieve field emission from tungsten, a widely used field emitter, such small voltages are highly advantageous. There are several materials which exhibit negative electron affinity, but almost all of these materials are alkali metal based. Alkali metals are quite sensitive to atmospheric conditions and tend to decompose when exposed to air or moisture. Additionally, alkali metals have low melting points, typically below 1000°C, which may be unsuitable in certain applications.

For a full understanding of the prior art related to the present invention, certain attributes of diamond must also be discussed. Recently, it has been experimentally confirmed that the (111) surface of diamond crystal has an electron affinity of -0.7+/-0.5 electron volts, showing it to possess negative electron affinity. A common conception about diamonds is that they are very expensive to fabricate. This is not always the case, however. Newly invented plasma chemical vapor deposition processes appear to be promising ways to bring down the cost of producing high quality diamond thin films. For instance, high fidelity audio speakers with diamond thin films as vibrating cones are already commercially available. It should also be noted that diamond thin films cost far less than the high quality diamonds used in jewelry.

Diamond cold cathodes have been reported by Geis et al. in "Diamond Cold Cathode", IEEE Electron Device Letters, Vol. 12, No. 8, August 1991, pp. 456-459; and in "Diamond Cold Cathodes", Applications of Diamond Films and Related Materials, Tzeng et al. (Editors), Elsevier Science Publishers B. V., 1991, pp. 309-310. The diamond cold cathodes are formed by fabricating mesa-etched diodes using carbon ion implantation into p-type diamond substrates. Geis et al. indicate that the diamond can be doped either n- or p-type. In fact, several methods show promise for fabricating n-type diamond, such as bombarding the film with sodium, nitrogen or lithium during growth. However, in current practice it is extremely difficult to fabricate n-type diamond and efforts for n-type doping usually result in p-type diamond. Furthermore, p-type doping fails to take full advantage of the negative electron affinity effect, and pure or undoped diamond is insulating and normally charges up to prevent emission.

From the foregoing, there is a clear need for a thermodynamically stable material with negative electron affinity for use as a field emitter tip.

The present invention utilizes the extraordinary properties of diamond to provide a thermally stable negative electron affinity tip for a field emitter.

An object of the present invention is a process for fabricating large area field emitters with sharp sub-micron features without requiring photolithography.

Another object of the present invention is to provide a field emitter which requires only a relatively small voltage for field emission to occur.

Still another object of the present invention is a process for fabricating field emitters which uses relatively few steps.

A feature of the present invention is a field emitter composed of a conductive metal and a diamond emission tip with negative electron affinity in ohmic contact with and protruding above the conductive metal.

Another feature of the present invention is a method of fabricating a field emitter by coating a substrate with a diamond film having negative electron affinity and a top surface with spikes and valleys, depositing a conductive metal on the diamond film, and etching the metal to expose portions of the spikes without exposing the valleys, thereby forming diamond emission tips which protrude above the conductive metal.

A still further feature of the present invention is the use of an undoped insulating diamond emission tip which protrudes above a conductive metal by a height less than the mean free path of electrons in the tip thereby allowing the electrons to ballistically tunnel through the tip.

These and other objects, features and advantages of the present invention will be further described and more readily apparent from a review of the detailed description and preferred embodiments which follow.

The following detailed description of the preferred embodiments can best be understood when read in conjunction with the following drawings, wherein:

FIGS. 1A-1E show cross-sectional views of successive stages of fabricating a field emitter in accordance with one embodiment of the present invention, and

FIG. 2 shows an elevational perspective view of a field emitter of the present invention.

Referring now to the drawings wherein depicted elements are not necessarily shown to scale and wherein like or similar elements are designated by the same reference numeral through the several views, and more particularly to FIGS. 1A-1E, there are shown successive cross-sectional views of a field emitter generally designated 10 according to a particularly preferred embodiment of the invention.

With reference now to FIG. 1A, a large area substrate 12 is provided. Substrate 12 is preferably glass and quartz, although other materials can be used, the requirement being they provide a base upon which a thin film of diamond can be deposited.

Referring now to FIG. 1B, a thin film of diamond 14 with negative electron affinity is coated on substrate 12. Diamond film 14 is preferably 500 to 5,000 angstroms thick which precludes the use of natural diamond. Further, diamond film 14 is undoped and insulating. The preferred method of coating the thin diamond film 14 is by chemical vapor deposition (CVD) but other methods such as sputtering, laser deposition and ion beam deposition are also suitable. The raw materials for diamond CVD are a hydrocarbon (usually methane (CH4)) and hydrogen, and diamond CVD systems are similar to standard silicon oxide CVD systems. During CVD the combination of high temperature and plasma decomposes the hydrocarbon gas and activates high energy carbon atoms. The high energy carbon atoms bombard substrate 12 and form a carbon film thereon. In addition, the high energy bombardment causes the lattice configuration of the deposited carbon atoms to change. Various carbon lattice structures, while composed of the same material, form highly differing structures, such as carbon soot, graphite, and diamond. In the present invention, the deposited carbon atoms are bonded to four other carbon atoms. This lattice forms a diamond film on the substrate. Further details of CVD diamond films are described in the entire issue of the Journal of Materials Research, Vol. 5, No. 11, November 1990, which is incorporated herein by reference.

Diamond films can assume several orientations, such as (100), (110) and (111). The preferred orientation for diamond film 14 is (111) for several reasons. The (111) orientation provides the sharpest vertical features, shown as spikes 16 surrounded by valleys 18 on top surface 20 of diamond film 14. The (111) orientation also grows the fastest in the vertical direction. Moreover, it has been experimentally confirmed that the (111) surface of diamond has a negative electron affinity in the range of -1.2 to -0.2 electron volts. Nonetheless, other orientations can be used in the present invention as long as the diamond film retains negative electron affinity. The desired orientation of diamond can be obtained by applying the appropriate temperature during CVD.

The thermal conductivity of diamond film 14 is relatively high, for instance at least five times that of copper. However, since diamond film 14 contains more defects than natural diamond, the thermal conductivity of diamond film 14 is approximately less than half that of natural diamond.

Referring now to FIG. 1C, the next step of the present invention is to deposit a conductive metal over the diamond film. Sputtering and evaporation are the preferred deposition techniques, with sputtering most preferred due to the low contamination and high integrity of the deposited metal. Further details of thin film technology are well known in the art; see, for instance, Maissel and Glang, Handbook of Thin Film Technology, 1983 Reissue, McGraw-Hill, New York, N.Y. Preferred metals are tungsten and titanium since they make good ohmic contact with diamond, with titanium most preferred. As may be seen, conductive metal 22 is deposited over diamond film 14 to form a metal layer thereon wherein conductive metal portions 24 cover spikes 16 and conductive metal portions 26 cover valleys 18. Conductive metal 22 preferably forms a uniform metal coating approximately 500 to 3,000 angstroms thick.

With reference now to FIG. 1D, an etch is applied to remove some but not all of conductive metal 22 in order to expose portions 28 of spikes 16 without exposing valleys 18. The exposed diamond portions 28 serve as raised field emission tips 30. The preferred etch is ion milling, although wet etching is also suitable, as is plasma etching or a combination thereof. In the present embodiment, two important features help assure diamond tips 30 are exposed while at least some metal 26 remains to cover valleys 18. First, the sharpness of spikes 16 compared to the flatness of valleys 18 allows metal 24 on spikes 16 to etch at a faster rate than metal 26 on valleys 18. This results in the non-etched metal having a substantially planar top surface 34. Second, conductive metal 22 has a faster etch rate than diamond 14 to help assure that the diamond will protrude above the conductive metal 22 after the etch is discontinued. For instance, when 500 electron volts of argon ions are used for sputter etching, the sputter yield (i.e., for an incoming atom, how many atoms are etched off) of diamond is 0.12 as compared to 0.51 for titanium and 1.18 for chromium.

When the etching is finished, emission tips 30 with peaks 36 protrude above non-etched metal top surface 34 by a height 38 less than the mean free path of electrons in diamond 14 to assure the desired field emission can later occur. That is, as long as the injection surface 34 is closer to the ejection point 36 than the mean free path of electrons in the emission tip 30, then statistically the electron emission shall occur due to the ballistic tunneling of electrons through the diamond. Applicant is not aware of the mean free path for electrons in CVD diamond, but estimates the distance to be in the range of 20 to 50 angstroms, which encompasses most materials, and almost certainly in the range of 10 to 100 angstroms. Therefore, vertical distance 38 is preferably no larger than 50 angstroms, more preferably no larger than approximately 20 angstroms, and most preferably no larger than approximately 10 angstroms. The horizontal space 40 between peaks 36 is preferably less than 1 micron, thus providing fine features with high emission tip density that are difficult to realize with photolithography based processes.

Referring now to FIG. 1E, it is critical that a low resistance connection between the conductive metal 22 and diamond film 14, commonly known as an "ohmic contact" be formed since higher contact resistance generates greater heat during field emission operation. An ohmic contact may arise during the step of depositing metal 22 on diamond 14, particularly if titanium or tungsten is sputter deposited. However, if an ohmic contact is not present, or if a better ohmic contact is desired, then an annealing step either before or after the etching step may be advantageous. For instance, field emitter 10 can be subjected to a 400°C to 500°C bake for approximately 10 minutes. This forms a 10 angstrom thick alloy 42 of diamond 14 and conductor 22 at the interface therebetween. Alloy 42 maintains a low resistance ohmic contact between diamond film 14 and conductor 22.

Referring now to FIG. 2, there is seen a perspective view of the field emitter 10 after fabrication is completed.

Other such possibilities should readily suggest themselves to persons skilled in the art. For example, a simpler technique would be to deposit a thin layer of diamond on top of a titanium layer and then anneal the layers at a high temperature to form an ohmic contact therebetween. However, this approach is not considered of practical importance since the number of diamond nucleation sites (and thus emission tips) would be difficult to control. In addition, only a generic structure of a field emitter has been shown herein. No attempt has been made to describe the various structures and devices in which such an emitter may be used.

The method of making the field emitter of the present invention is apparent from the foregoing description.

The present invention, therefore, is well adapted to carry out the objects and attain the ends and advantages mentioned, as well as others inherent therein. While presently preferred embodiments of the present invention have been described for the purpose of disclosure, numerous other changes in the details of construction, arrangement of parts, compositions and materials selection, and processing steps can be carried out without departing from the spirit of the present invention which is intended to be limited only by the scope of the appended claims.

Kumar, Nalin

Patent Priority Assignee Title
10019760, Mar 20 2015 Bank of America Corporation System for utilizing a retirement score to receive benefits
10032223, Mar 20 2015 Bank of America Corporation System for account linking and future event integration into retirement score calculation
10049406, Mar 20 2015 Bank of America Corporation System for sharing retirement scores between social groups of customers
10249003, Mar 20 2015 Bank of America Corporation System for sharing retirement scores between social groups of customers
10262372, Mar 20 2015 Bank of America Corporation System for utilizing a retirement score to receive benefits
10628887, Mar 20 2015 Bank of America Corporation System for account linking and future event integration into retirement score calculation
5491348, May 14 1993 Kobe Steel USA, Inc. Highly-oriented diamond film field-effect transistor
5493131, May 14 1993 Kobe Steel USA, Inc. Diamond rectifying element
5505649, Jul 27 1994 Samsung Display Devices Co., Ltd. Field emission display device and method for producing such display device
5545946, Dec 17 1993 Motorola Field emission display with getter in vacuum chamber
5552613, Sep 24 1993 Sumitomo Electric Industries, Ltd. Electron device
5600200, Jun 02 1993 APPLIED NANOTECH HOLDINGS, INC Wire-mesh cathode
5601966, Nov 04 1993 SI DIAMOND TECHNOLOGY, INC Methods for fabricating flat panel display systems and components
5612712, Mar 16 1992 APPLIED NANOTECH HOLDINGS, INC Diode structure flat panel display
5614353, Nov 04 1993 SI DIAMOND TECHNOLOGY, INC Methods for fabricating flat panel display systems and components
5616061, Jul 05 1995 Advanced Vision Technologies, Inc Fabrication process for direct electron injection field-emission display device
5644190, Jul 05 1995 Advanced Vision Technologies, Inc Direct electron injection field-emission display device
5647998, Jun 13 1995 Advanced Vision Technologies, Inc Fabrication process for laminar composite lateral field-emission cathode
5652083, Nov 04 1993 SI DIAMOND TECHNOLOGY, INC Methods for fabricating flat panel display systems and components
5663611, Feb 08 1995 GE Aviation UK Plasma display Panel with field emitters
5675216, Mar 16 1992 APPLIED NANOTECH HOLDINGS, INC Amorphic diamond film flat field emission cathode
5679043, Mar 16 1992 APPLIED NANOTECH HOLDINGS, INC Method of making a field emitter
5686791, Jun 02 1993 APPLIED NANOTECH HOLDINGS, INC Amorphic diamond film flat field emission cathode
5702281, Apr 20 1995 Transpacific IP Ltd Fabrication of two-part emitter for gated field emission device
5703380, Jun 13 1995 Advanced Vision Technologies, Inc Laminar composite lateral field-emission cathode
5703435, Jun 02 1993 APPLIED NANOTECH HOLDINGS, INC Diamond film flat field emission cathode
5710478, Aug 25 1995 Agency of Industrial Science & Technology, Ministry of International Field emitter having source, channel, and drain layers
5723954, Apr 14 1995 Lawrence Livermore National Security LLC Pulsed hybrid field emitter
5736810, Oct 28 1994 International Business Machines Corporation Non-evacuated lateral fed employing emitter-anode spacing less than mean free path distance of an electron in air
5751097, Apr 30 1996 International Business Machines Corporation Lateral field emission devices for display elements and methods of fabrication
5763997, Mar 16 1992 APPLIED NANOTECH HOLDINGS, INC Field emission display device
5777427, Oct 05 1994 MATSUSHITA ELECTRIC INDUSTRIAL CO , LTD Electron emission cathode having a semiconductor film; a device including the cathode; and a method for making the cathode
5811916, Oct 31 1994 Bell Semiconductor, LLC Field emission devices employing enhanced diamond field emitters
5821680, Oct 17 1996 Sandia Corporation Multi-layer carbon-based coatings for field emission
5821685, May 13 1996 Motorola, Inc. Display with UV-light emitting phosphor
5844252, Sep 24 1993 SUMITOMO ELECTRIC INDUSTRIES, LTD Field emission devices having diamond field emitter, methods for making same, and methods for fabricating porous diamond
5857882, Feb 27 1996 Sandia Corporation Processing of materials for uniform field emission
5861707, Nov 07 1991 SI DIAMOND TECHNOLOGY, INC Field emitter with wide band gap emission areas and method of using
5965971, Jan 19 1993 Kypwee Display Corporation Edge emitter display device
5969363, Apr 11 1997 Hitachi, LTD Method for processing electron beam sources
5969473, Apr 20 1995 Transpacific IP Ltd Two-part field emission structure
5984752, Oct 05 1994 Matsushita Electric Industrial Co., Ltd. Electron emission cathode; an electron emission device, a flat display, a thermoelectric cooling device incorporating the same; and a method for producing the electron emission cathode
6011269, Apr 10 1998 Applied Materials, Inc Shaped shadow projection for an electron beam column
6023126, Jan 19 1993 Kypwee Display Corporation Edge emitter with secondary emission display
6113451, Jun 30 1997 The United State of America as represented by the Secretary of the Navy Atomically sharp field emission cathodes
6127773, Mar 16 1992 APPLIED NANOTECH HOLDINGS, INC Amorphic diamond film flat field emission cathode
6184611, Mar 10 1997 SUMITOMO ELECTRIC INDUSTRIES, LTD Electron-emitting element
6201342, Jun 30 1997 The United States of America as represented by the Secretary of the Navy; UNITED STATES OF AMERICA, THE, AS REPRESENTED BY THE SECRETARY OF THE NAVY Automatically sharp field emission cathodes
6340860, Apr 11 1997 Hitachi, Ltd. Method of manufacturing electron beam emitter having an electron beam emitting axis coincided with crystal axis
6356014, Mar 27 1997 Entegris, Inc Electron emitters coated with carbon containing layer
6504311, Mar 25 1996 SI DIAMOND TECHNOLOGY, INC Cold-cathode cathodoluminescent lamp
6534923, Jul 13 2001 Microwave Power Technology Electron source
6629869, Mar 16 1992 APPLIED NANOTECH HOLDINGS, INC Method of making flat panel displays having diamond thin film cathode
8101130, Sep 15 2006 Applied Nanotech Holdings, Inc. Gas ionization source
9830660, Mar 20 2015 Bank of America Corporation System for augmenting a retirement score with health information
Patent Priority Assignee Title
2959704,
3894332,
3947716, Aug 27 1973 The United States of America as represented by the Secretary of the Army Field emission tip and process for making same
3970887, Jun 19 1974 ST CLAIR INTELLECTUAL PROPERTY CONSULTANTS, INC A CORP OF MI Micro-structure field emission electron source
3998678, Mar 22 1973 Hitachi, Ltd. Method of manufacturing thin-film field-emission electron source
4084942, Aug 27 1975 Ultrasharp diamond edges and points and method of making
4139773, Nov 04 1977 Fei Company Method and apparatus for producing bright high resolution ion beams
4164680, Aug 27 1975 Polycrystalline diamond emitter
4307507, Sep 10 1980 The United States of America as represented by the Secretary of the Navy Method of manufacturing a field-emission cathode structure
4350926, Jul 28 1980 The United States of America as represented by the Secretary of the Army Hollow beam electron source
4498952, Sep 17 1982 Condesin, Inc. Batch fabrication procedure for manufacture of arrays of field emitted electron beams with integral self-aligned optical lense in microguns
4663559, Sep 17 1982 Field emission device
4685996, Oct 14 1986 Method of making micromachined refractory metal field emitters
4687938, Dec 17 1984 Hitachi, Ltd. Ion source
4855636, Oct 08 1987 Micromachined cold cathode vacuum tube device and method of making
4933108, Apr 13 1978 Emitter for field emission and method of making same
4943343, Aug 14 1989 BOEING ELECTRON DYNAMIC DEVICES, INC ; L-3 COMMUNICATIONS ELECTRON TECHNOLOGIES, INC Self-aligned gate process for fabricating field emitter arrays
4964946, Feb 02 1990 The United States of America as represented by the Secretary of the Navy; UNITED STATES OF AMERICA, THE, AS REPRESENTED BY THE SECRETARY OF THE NAVY Process for fabricating self-aligned field emitter arrays
5019003, Sep 29 1989 Motorola, Inc. Field emission device having preformed emitters
5129850, Aug 20 1991 MOTOROLA SOLUTIONS, INC Method of making a molded field emission electron emitter employing a diamond coating
5138237, Aug 20 1991 Motorola, Inc. Field emission electron device employing a modulatable diamond semiconductor emitter
5141460, Aug 20 1991 MOTOROLA SOLUTIONS, INC Method of making a field emission electron source employing a diamond coating
5180591, Jul 11 1990 ALZA Corporation Delivery device with a protective sleeve
//
Executed onAssignorAssigneeConveyanceFrameReelDoc
Nov 24 1992Microelectronics and Computer Technology Corporation(assignment on the face of the patent)
Dec 16 1997MICROELECTRONICS AND COMPUTER TECHNOLOGY CORP SI DIAMOND TECHNOLOGY, INC ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0090970738 pdf
Date Maintenance Fee Events
Sep 12 1994ASPN: Payor Number Assigned.
Aug 11 1998REM: Maintenance Fee Reminder Mailed.
Aug 21 1998M283: Payment of Maintenance Fee, 4th Yr, Small Entity.
Aug 21 1998M286: Surcharge for late Payment, Small Entity.
Aug 28 1998SM02: Pat Holder Claims Small Entity Status - Small Business.
Feb 25 2002M184: Payment of Maintenance Fee, 8th Year, Large Entity.
Feb 21 2006M1553: Payment of Maintenance Fee, 12th Year, Large Entity.
Nov 20 2009ASPN: Payor Number Assigned.
Nov 20 2009RMPN: Payer Number De-assigned.


Date Maintenance Schedule
Aug 23 19974 years fee payment window open
Feb 23 19986 months grace period start (w surcharge)
Aug 23 1998patent expiry (for year 4)
Aug 23 20002 years to revive unintentionally abandoned end. (for year 4)
Aug 23 20018 years fee payment window open
Feb 23 20026 months grace period start (w surcharge)
Aug 23 2002patent expiry (for year 8)
Aug 23 20042 years to revive unintentionally abandoned end. (for year 8)
Aug 23 200512 years fee payment window open
Feb 23 20066 months grace period start (w surcharge)
Aug 23 2006patent expiry (for year 12)
Aug 23 20082 years to revive unintentionally abandoned end. (for year 12)